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6 in total

1. Primary adrenal insufficiency in a child with a mitochondrial DNA deletion.

Authors: C Bruno; C Minetti; Y Tang; P J Magalhães; F M Santorelli; S Shanske; M Bado; G Cordone; R Gatti; S DiMauro
Journal: J Inherit Metab Dis Date: 1998-04 Impact factor: 4.982

2. Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.

Authors: J Egger; B D Lake; J Wilson
Journal: Arch Dis Child Date: 1981-10 Impact factor: 3.791

3. "Bartter-like" phenotype in Kearns-Sayre syndrome.

Authors: Francesco Emma; Carla Pizzini; Alessandra Tessa; Silvia Di Giandomenico; Andrea Onetti-Muda; Filippo M Santorelli; Enrico Bertini; Gianfranco Rizzoni
Journal: Pediatr Nephrol Date: 2005-12-29 Impact factor: 3.714

4. Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia.

Authors: A Quade; S Zierz; D Klingmüller
Journal: Clin Investig Date: 1992-05

5. Congestive heart failure due to mitochondrial cardiomyopathy in Kearns-Sayre syndrome.

Authors: F X Kleber; J W Park; G Hübner; A Johannes; D Pongratz; E König
Journal: Klin Wochenschr Date: 1987-05-15

Review 6. Mitochondrial DNA mutations in renal disease: an overview.

Authors: Larissa P Govers; Hakan R Toka; Ali Hariri; Stephen B Walsh; Detlef Bockenhauer
Journal: Pediatr Nephrol Date: 2020-01-10 Impact factor: 3.714

6 in total